US20070265488A1 - After-loader for positioning implants for needle delivery in brachytherapy and other radiation therapy - Google Patents

Abstract

In one embodiment an after-loader for providing an implant to a hollow needle, the after-loader comprising a body having a distal end including a bevel for receiving a hub of a seed lock needle, and a bore therethrough for receiving a hub of a MICK® needle; a proximal end having a funnel shaped opening; a shield adapted to be provided over the body; and wherein the distal end further includes a taper along a portion of a distance from the distal end to the proximal end for providing a friction fit to a shield. This abstract is not intended to be a complete description of the invention.

Description

CLAIM OF PRIORITY
• This application claims priority to the following U.S. Provisional Applications, which are incorporated herein by reference.
• U.S. Provisional Application Ser. No. 60/799,161, entitled “After-loader for Positioning Implants for Needle Delivery in Brachytherapy and Other Radiation Therapy,” by Gary Lamoureux et al., filed May 9, 2006 (Attorney Docket No. WORLD-01026US0);
• U.S. Provisional Application Ser. No. 60/847,834, by Gary Lamoureux et al., entitled “After-loader for Positioning Implants for Needle Delivery in Brachytherapy and Other Radiation Therapy,” filed Sep. 28, 2006 (Attorney Docket No. WORLD-1026US1).
FIELD OF THE INVENTION
• This invention relates to radiotherapy. More particularly, it relates to applicators for positioning implants e.g., for use in brachytherapy.
BACKGROUND
• Brachytherapy is a general term covering medical treatment which involves placement of radioactive sources near a diseased tissue and can involve the temporary or permanent implantation or insertion of radioactive sources into the body of a patient. The radioactive sources are located in proximity to the area of the body which is being treated. A high dose of radiation can thereby be delivered to the treatment site with relatively low doses of radiation to surrounding or intervening healthy tissue. Exemplary radioactive sources include radioactive seeds, radioactive rods and radioactive coils.
• Brachytherapy has been used or proposed for use in the treatment of a variety of conditions, including arthritis and cancer. Exemplary cancers that can be treated using brachytherapy include breast, brain, liver and ovarian cancer and especially prostate cancer in men. For a specific example, treatment for prostate cancer can involve the temporary implantation of radioactive sources (e.g., rods) for a calculated period, followed by the subsequent removal of the radioactive sources. Alternatively, radioactive sources (e.g., seeds) can be permanently implanted in the patient and left to decay to an inert state over a predictable time. The use of temporary or permanent implantation depends on the isotope selected and the duration and intensity of treatment required.
• Permanent implants for prostate treatment include radioisotopes with relatively short half lives and lower energies relative to temporary seeds. Exemplary permanently implantable sources include iodine-125, palladium-103 or cesium-131 as the radioisotope. The radioisotope can be encapsulated in a biocompatible casing (e.g., a titanium casing) to form a “seed” which is then implanted. Temporary implants for the treatment of prostate cancer may involve iridium-192 as the radioisotope. For temporary implants, radioactive rods are often used.
• Conventional radioactive seeds are typically smooth sealed containers or capsules of a biocompatible material, e.g., titanium or stainless steel, containing a radioisotope within the sealed chamber that permits radiation to exit through the container/chamber walls. Other types of implantable radioactive sources for use in radiotherapy are radioactive rods and radioactive coils, as mentioned above.
• Preferably, the implantation of radioactive sources for brachytherapy is carried out using minimally-invasive techniques such as, e.g., techniques involving needles and/or catheters. It is possible to calculate a desired location for each radioactive source which will give the desired radiation dose profile. This can be done using knowledge of the radioisotope content of each source, the dimensions of the source, accurate knowledge of the dimensions of the tissue or tissues in relation to which the source is to be placed, plus knowledge of the position of the tissue relative to a reference point. The dimensions of tissues and organs within the body for use in such dosage calculations can be obtained prior to or during placement of the radioactive sources by using conventional diagnostic imaging techniques including X-ray imaging, magnetic resonance imaging (MRI), computed tomography (CT) imaging, fluoroscopy and ultrasound imaging.
• During the placement of the radioactive sources into position, a surgeon can monitor the position of tissues such as the prostate gland using, e.g., ultrasound imaging or fluoroscopy techniques which offer the advantage of low risk and convenience to both patient and surgeon. The surgeon can also monitor the position of the relatively large needle used in implantation procedures using ultrasound or other imaging.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a side view of a hub of a seed lock needle.
• FIG. 2 is a side view of an embodiment of an after-loader in accordance with the present invention.
• FIG. 3 is a perspective view of the after-loader ofFIG. 2.
• FIG. 4A is an embodiment of a distal end plug for use with the after-loader ofFIG. 2;FIG. 4B is an embodiment of a proximal end plug for use with the after-loader ofFIG. 2;FIG. 4C is an alternative embodiment of a distal end plug for use with the after-loader ofFIG. 2;FIG. 4D is an alternative embodiment of a proximal end plug for use with the after-loader ofFIG. 2.
• FIG. 5 is a side view of the after-loader ofFIG. 2 with the distal end plug and proximal end plug in place.
• FIG. 6 is a side view of the after-loader ofFIG. 2 with shielding arranged over a portion of the after-loader.
• FIG. 7A is a cross-sectional side view of the after-loader ofFIG. 1 mated with a needle, and having a stylet disposed within the after-loader and needle;FIG. 7B is a cross-sectional side view of the after-loader ofFIG. 2 mated with a needle, and having a stylet disposed within the after-loader and needle.
• FIG. 8 is a flowchart of an embodiment of a method of using an after-loader in accordance with the present invention.
• FIG. 9 is a flowchart of an alternative embodiment of a method of using an after-loader in accordance with the present invention.
DETAILED DESCRIPTION
• Brachytherapy typically employs a hollow needle that is insertable through a template and into a patient's body. A typical template used to guide and/or inform the positioning of hollow needles at the surgical site can provide access to more than one hundred locations. The number of locations can be so numerous that a typical pitch between needle access points can include a pitch of 5 mm.
• One or more implants are provided to the hollow needle for delivery at a surgical site. A distal end of the hollow needle is typically inserted to the desired depth, thus at least one of the implant is typically urged to approximately the proximal end of the hollow needle. The implants can include a radioactive source. The radioactive source can be a radioactive seed, a radioactive rod, or a radioactive coil, but is not limited thereto. The radioactive source can further be an anchor seed, which is a seed having an outer shape and/or outer coating adapted to resist movement once implanted at a desired location within the patient, for example, as disclosed in U.S. patent application Ser. No. 11/187,411, entitled “Implants for Use in Brachtherapy and Other Radiation Therapy That Resist Migration and Rotation,” filed Jul. 22, 2005, which is incorporated herein by reference. Alternatively, the implant can be some other object and need not be radioactive, e.g. the implant can be a spacer, or a marker. For reasons of convenience, embodiments will be described with reference to a “seed,” however it will be understood that embodiments can additionally or alternatively be used with any implant.
• A hollow needle for use in Brachytherapy can include a MICK® needle or alternatively some other hollow needle, such as a seed lock needle. It has become a relatively common practice for physicians to employ needles other than MICK® needles; however, MICK® needles continue to be in popular use. A MICK® needle includes a hub positioned at a proximal end, the hub being a generally simple cylinder in shape. Referring toFIG. 1, aseed lock needle4 differs from a MICK® needle in that the hollow needle2 is coupled to ahub6 having an enlarged diameter with a funneledproximal end8 that typically screws onto a syringe. The funneledproximal end8 allows a more forgiving tolerance for inserting implants into the hollow needle2. However, tools for expediting and/or simplifying the loading process of the implant within the hollow needle are typically compatible with only one of multiple types of needles.
• Referring toFIGS. 2,3 and5 through7B, embodiments of after-loaders100 in accordance with the present invention can simplify and/or expedite loading of implants into a needle. The after-loader100 can accommodate a MICK® needle160 (shown inFIG. 7B) within abore120 of adistal end110 of the after-loader100, or alternatively a seed lock needle4 (shown inFIG. 7A), providing flexibility in hollow needle choice. Thedistal end110 can include an enlarged diameter tapering at an angle θ from its largest diameter toward the proximal end of the after-loader100 at some small angle. In accordance with an embodiment, the maximum diameter of the after-loader100 near thedistal end110 is 3/16″ necking down at a 5 degree angle. The purpose of this taper is to accept a shield150 (shown inFIG. 6) over the outside of the after-loader100, and to further provide a friction fit to lock the shield over the after-loader100, the friction fit being attributable to the increase in diameter toward thedistal end110. Theshield150 is positioned around the after-loader100 to reduce or minify an amount of radiation that escapes from the after-loader100 where the implants placed in the after-loader100 are radioactive. The after-loader100 itself can be formed using a transparent plastic, for example by molding, but is not limited thereto. Where the after-loader100 is formed of a plastic, the after-loader100 does not sufficiently restrict radiation from escaping the after-loader100; therefore, shielding is employed to prevent leakage. Theshield150 can be formed of some material that sufficiently restricts the amount of radiation that escapes theshield150, such as stainless steel. In other embodiments, after-loaders100 of the present invention can be formed from a different material more opaque to radiation, such as stainless steel. In such embodiments a separate shield is not necessary.
• Referring toFIG. 7A, thenose118 of the after-loader100 is tapered at an angle α generally corresponding to an angle of the funneledproximal end8 of aseed lock needle4. Thus, an external angle of thenose end118 can be approximately 15 degrees in angle, in an embodiment wherein a typicalseed lock needle4 is to be accommodated. Thenose118 of the after-loader100 is positioned within the funneledproximal end8 so that the after-loader100 is removably mated with thehub6 of theseed lock needle4.
• Still further, thedistal end110 of the after-loader100 includes an enlarged diameter relative to thebody112 of the after-loader100, which roughly corresponds to a diameter of a hollow needle. As further shownFIG. 7B, thedistal end110 is such that the enlarged diameter can accommodate thehub162 of aMICK® needle160, and in an embodiment thedistal end110 has a length generally sufficient to receive thehub162 of theMICK® needle160. Thus, the after-loader100 can be removably mated with a MICK® needle or a seed lock needle, at the option of the physician. The funneled shape of thedistal end110 also accommodates a distal end plug180 (shown inFIGS. 4A and 5) inserted into thedistal end110, thedistal end plug180 functioning to hold implants positioned within the after-loader100 in place. Thedistal end plug180 prevents implants from falling out of the after-loader100, and further can be employed to block radiation from emitting from the end of the after-loader100. It should be noted that thedistal end plug180 need not be shaped as shown inFIGS. 4A and 5. Thedistal end plug180 need only be shaped so as to function to accommodate the implant within the after-loader100. For example, where radiation emission from the longitudinal ends of implant is not a concern, the end plug need not function to block radiation. Thus, in some embodiments, for example, a distal end plug280 as shown inFIG. 4C can be employed to resist undesired movement within the after-loader100 and provide for removal, which as shown is accomplished by way of a textured surface281.
• An opening at theproximal end130 of the after-loader100 can be funneled having an angle β to simplify insertion into abore114 of thebody112 of the after-loader100 an implant, or a stylet (also referred to herein as a push-rod). For example, the funnel can cause an increase in diameter at a 10 degree angle. The funneled shape of the opening at theproximal end130 also accommodates a proximal end plug182 (shown inFIGS. 4B and 5) inserted into theproximal end130, theproximal end plug182 functioning to hold implants positioned within the after-loader100 in place. Theproximal end plug182 prevents implants from falling out of the after-loader100, and further can be employed to block radiation from emitting from the end of the after-loader100. Thedistal end plug180 andproximal end plug182 shown inFIGS. 4A-5 are merely embodiments of plugs for use with after-loaders in accordance with the present invention. In other embodiments, some other style of plug can be employed to retain an implant with an after-loader. In still other embodiments, plugs for use with the after-loader of the present invention can be integrally formed with an implant housed within the after-loader. Theproximal end plug182 need only be shaped so as to function to accommodate the implant within the after-loader100. For example, where radiation emission from the longitudinal ends of the implant is not a concern, the end plug need not function to block radiation. Thus, in some embodiments, a distal end plug282 as shown inFIG. 4D can be employed to resist undesired movement within the after-loader100 and provide for removal, which as shown is accomplished by way of a textured surface283.
• Referring toFIG. 8, the distal end of a hollow needle is positioned at the desired location within a patient's body (e.g. by way of a template) prior to use of the after-loader100 (Step100). The hub of the hollow needle is mated with thedistal end110 of the after-loader100 (Step102), either by way of thetapered nose118 or thebore120 of thedistal end110. With the implant positioned within the after-loader100 a stylet170 (shown inFIGS. 7A and 7B) is inserted into theproximal end130 of the after-loader100 (Step104) and is urged toward the distal end of the needle until the implant is positioned at the desired location (Step106). Thestylet170 for use with the after-loader100 can be sufficient in length to accommodate both the needle and the after-loader100, which are retracted while thestylet170 is held in position so that the implant is deposited at a desired location (Step108). Referring toFIG. 9, alternatively, a stylet of less than sufficient length to accommodate both the needle and the after-loader100 can be employed. When such a stylet is used, the stylet can urge the implant from the after-loader100 to the hollow needle (Step206). The stylet can then be removed, and the after-loader100 disconnected (Step208). Thestylet170 can then be reinserted into the hub of the needle to urge the implant to the desired location (Step210). The needle can then be retracted with the stylet held in position so that the implant is deposited at a desired location (Step212).
• As mentioned, the after-loader100 can be employed for use with a single seed, an anchor seed, multiple seeds with or without spacers between adjacent seeds, strands, a radioactive rod, or a radioactive coil, a marker, or some other implantable device. A strand can include a plurality of radioactive sources spaced apart from one another, e.g. in accordance with a treatment plan.
• In further embodiments of after-loaders in accordance with the present invention, the after-loaders100 can be pre-loaded with strands, loose seeds and spacers, or other implants so that the after-loader can be selected by the physician and used without loading by the physicians. Pre-configured strands, and other implants can be loaded into the after-loader100 off-site and fitted with plugs at theproximal end130 and the plugs to hold the ends in, and then shipped to the user and assigned to certain patients. Thus, the proper treatment can be determined as part of a pre-plan. In such embodiments, the after-loader would include shielding securely fitted to the outside surface of the after-loader100. Such pre-loaded after-loaders can simplify and expedite the implantation process. Further, such pre-loaded after-loaders100 offer benefits to hospitals or clinics that strive to minify the amount of handling of the implants performed by staff. It is also possible for a physician to load seeds, strands, or other implants into the after-loaders100 before needles are inserted into a patient. As will be appreciated, and which can be extrapolated from the embodiments described, the after-loaders100 can be longer or shorter in length as needed. For example, where an implant appropriate for a treatment plan is an anchor seed, the after-loaders100 can have a length appropriate to the implant.
• The after-loader100 can include a diameter that, at a maximum, is at least 5 mm in size to generally match the pitch of a typical template. However, in other embodiments, the after-loader100 can be larger or smaller in diameter.
• The previous description of the preferred embodiments is provided to enable any person skilled in the art to make or use the embodiments of the present invention. While the invention has been particularly shown and described with reference to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention.

Claims (18)

1. An after-loader for providing an implant to a hollow needle, the after-loader comprising:

a body having a distal end and a proximal end, the distal end including a bevel and a bore;

wherein the bevel is adapted to receive a hub of a first type of brachytherapy needle and the bore is adapted to receive a hub of a second type of brachytherapy needle.

2. The after-loader ofclaim 1, wherein:

the bore is a first bore; and

further comprising a second bore extending through the after-loader; and

wherein a portion of the second bore has an expanding funnel shape toward the proximal end.

3. The after-loader ofclaim 1, further comprising:

A radiation shield adapted to be provided over at least a portion of the body; and

wherein the distal end further includes a taper along a portion of a distance from the distal end to the proximal end for providing a friction fit to the shield.

4. The after-loader ofclaim 2, wherein the second bore is narrower than the first bore.

5. The after-loader ofclaim 1, wherein:

the bevel is adapted to receive a hub of a seed lock needle; and

the bore is adapted to receive a hub of a MICK needle.

6. The after-loader ofclaim 2, wherein the second bore is adapted to receive a stylet.

7. A system for positioning implants within a body of a patient, the system comprising:

a needle having a hub;

an afterloader including a body, the body having:

a distal end including a bevel and a first bore;

a proximal end; and

a second bore extending approximately from the proximal end to the first bore;

wherein the bevel and the first bore are selectable for receiving a hub of a needle; and

a stylet receivable within the second bore.

8. The system ofclaim 7, wherein a portion of the second bore has an expanding funnel shape toward the proximal end.

9. The system ofclaim 7, further comprising:

a radiation shield adapted to be provided over at least a portion of the body; and

wherein the distal end further includes a taper along a portion of a distance from the distal end to the proximal end for providing a friction fit to the shield.

10. The system ofclaim 7, wherein the second bore is narrower than the first bore.

11. The system ofclaim 7, wherein:

the bevel is adapted to receive a hub of a seed lock needle; and

the first bore is adapted to receive a hub of a MICK needle.

12. The system ofclaim 7, wherein:

the stylet has a distal end and a proximal end;

the proximal end includes a hub adapted to be gripped; and

the distal end of the stylet has sufficient length to extend in a distal direction through the needle and afterloader at least to a distal end of the needle.

13. A method for positioning an implant within a body of a patient, the method comprising:

positioning a hollow needle at a desired location within the body;

selecting an after-loader adapted to be mated with a hub of the needle so that the hub can be received over a distal end of the after-loader or within the distal end of the after-loader;

mating the hub of the hollow needle with a distal end of the after-loader;

inserting a stylet into the proximal end of the after-loader;

urging the stylet toward the distal end of the after-loader until the implant is loaded into the needle.

14. The method ofclaim 13, further comprising:

retracting the stylet from the after-loader;

separating the distal end of the after-loader from the hub of the hollow needle;

urging the stylet toward the distal end of the needle until the implant is positioned substantially at the distal end of the needle; and

retracting the needle with the stylet held in position so that the implant is deposited at the desired location.

15. The method ofclaim 13, further comprising:

urging the stylet toward the distal end of the needle until the implant is positioned substantially at the distal end of the needle; and

retracting the needle and after-loader with the stylet held in position so that the implant is deposited at the desired location.

16. An after-loader for providing an implant to a hollow needle, the after-loader comprising:

a body having a distal end and a proximal end and a bore extending therebetween;

at least one implant stored in the bore;

wherein the distal end is configured to be mated to a hub of a hollow needle;

wherein the proximal end is configured to accept a stylet.

17. The after-loader ofclaim 16, further comprising:

a pair of removable plugs to keep the at least one implant within the bore until the plugs are removed.

18. The after-loader ofclaim 16, further comprising:

a radiation shield adapted to be provided over at least a portion of the body; and

wherein the distal end further includes a taper along a portion of a distance from the distal end to the proximal end for providing a friction fit to the shield.

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